Zobrazeno 1 - 8 of 8 pro vyhledávání: '"Bérengère Cador"'
2
Immunoglobulin Abnormalities in Gaucher Disease: an Analysis of 278 Patients Included in the French Gaucher Disease Registry
Autor: Yann Nguyen, Dries Dobbelaere, Jérôme Stirnemann, Monia Bengherbia, Fabrice Camou, Samia Pichard, Karima Yousfi, Christine Serratrice, Agathe Masseau, Vanessa Leguy-Seguin, Marc G. Berger, Nadia Belmatoug, Dalil Hamroun, Bruno Fantin, Florent Lautredoux, Francis Gaches, Leonardo Astudillo, Anaïs Brassier, Bérengère Cador, Florence Dalbies, Yves-Marie Pers, Thierry Billette de Villemeur
Publikováno v: International Journal of Molecular Sciences
Volume 21
Issue 4
International Journal of Molecular Sciences, 2020, 21 (4), pp.1247. ⟨10.3390/ijms21041247⟩
International Journal of Molecular Sciences, Vol 21, Iss 4, p 1247 (2020)
International Journal of Molecular Sciences, Vol. 21, No 4 (2020) P. 1247
International Journal of Molecular Sciences, MDPI, 2020, 21 (4), pp.1247. ⟨10.3390/ijms21041247⟩
Gaucher disease (GD) is a rare lysosomal autosomal-recessive disorder due to deficiency of glucocerebrosidase
polyclonal gammopathy (PG) and/or monoclonal gammopathy (MG) can occur in this disease. We aimed to describe these immunoglobulin abnor
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90aee55c5e8ec2af6466291e46dc07c6
Zobrazit plný text záznamu
3
A Cross-Sectional Retrospective Study of Non-Splenectomized and Never-Treated Patients with Type 1 Gaucher Disease
Autor: Isabelle Durieu, Leonardo Astudillo, Ivan Bertchansky, Samia Pichard, Amina Berrahal, Nadia Belmatoug, Roseline Froissart, Catherine Caillaud, Monia Bengherbia, Jérôme Stirnemann, Vanessa Leguy Seguin, Karima Yousfi, Bérengère Cador, Marc G. Berger, Laure Swiader, Catherine Marcel, Claire de Moreuil, Bénédicte Hivert, Sébastien Humbert, Thierry Billette de Villemeur, Christine Serratrice, Brigitte Chabrol, Isabelle Hau Rainsard, Agathe Masseau, Fabrice Camou, Anaïs Brassier, Florence Dalbies
Publikováno v: Journal of Clinical Medicine, Vol. 9, No 8 (2020) P. 2343
Journal of Clinical Medicine
Journal of Clinical Medicine; Volume 9; Issue 8; Pages: 2343
Journal of Clinical Medicine, 2020, 9 (8), pp.2343. ⟨10.3390/jcm9082343⟩
Journal of Clinical Medicine, MDPI, 2020, 9 (8), pp.2343. ⟨10.3390/jcm9082343⟩
Journal of Clinical Medicine, Vol 9, Iss 2343, p 2343 (2020)
International audience; Patients with type 1 Gaucher disease (GD1) present thrombocytopenia, anemia, organomegaly, and bone complications. Most experts consider that the less aggressive forms do not require specific treatment. However, little is know
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25191cbc046a11eeca95291a613c0f1e
https://archive-ouverte.unige.ch/unige:145459
Zobrazit plný text záznamu
4
Étude des mucopolysaccharidoses en France : constitution de la cohorte RaDiCo-MPS
Autor: A.S. Guemann, Bérengère Cador, E. Klising, Anaïs Brassier, Brigitte Chabrol, P. Beze-Beyrie, E. Sacaze, François Feillet, S. Guéguen, T. Billette de Villemeur, M. Barth, Y. Nadjar, Nadia Belmatoug, Serge Amselem, Agathe Roubertie, S. Pichard, I. Dufaure Garé, l’équipe RaDiCo, Marc Tardieu, Bénédicte Héron
Publikováno v: Revue d'Épidémiologie et de Santé Publique. 69:S104-S105
Introduction Les mucopolysaccharidoses (MPS) sont des maladies de surcharge lysosomale : il s’agit de maladies genetiques rares (1/25 000 a 30 000 naissances). Ces maladies ont une evolution chronique, progressive et multisystemique avec des sympto
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::28dcd6e3e4295b073f2de8ee1bdf3c0e
https://doi.org/10.1016/j.respe.2021.05.034
Zobrazit plný text záznamu
5
NLRP3-associated autoinflammatory diseases: Phenotypic and molecular characteristics of germline versus somatic mutations
Autor: Noémie Lachaume, Fawaz Awad, Bruno Copin, Serge Amselem, Camille Louvrier, Emmanuelle Bourrat, Claire Jumeau, Philippe Duquesnoy, Sonia Karabina, Eman Assrawi, Bérengère Cador-Rousseau, Elma El Khouri, G. Grateau, William Piterboth, S. Georgin-Lavialle, Marie Legendre, Isabelle Melki, Irina Giurgea
Publikováno v: Journal of Allergy and Clinical Immunology
Journal of Allergy and Clinical Immunology, Elsevier, 2020, 145 (4), pp.1254-1261. ⟨10.1016/j.jaci.2019.11.035⟩
International audience; Background: NLRP3-associated autoinflammatory diseases (NLRP3-AIDs) include conditions of various severities, due to germline or somatic mosaic NLRP3 mutations.Objective: To identify mosaic- versus germline-specific NLRP3 muta
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8a2ad29a4cc963f3f6bd0f31ab7e1af
https://pubmed.ncbi.nlm.nih.gov/31816408
Zobrazit plný text záznamu
6
Monoclonal gammopathies and hypergammaglobulemia in Gaucher disease: an analysis from the French Gaucher disease registry
Autor: Marc G. Berger, Yann Nguyen, Nadia Belmatoug, Bruno Fantin, Florent Lautredoux, Jérôme Stirnemann, Dalil Hamroun, Karima Yousfi, Bérengère Cador, Bengherbia Monia
Publikováno v: 13th EWGGD Meeting
13th EWGGD Meeting, Jul 2019, Clermont-Ferrand, France
Objectives: To determine the risk factors, the clinical significance, and the evolution of monoclonal gammopathy (MG) and hypergammaglobulinemia (HG) in Gaucher disease (GD). Methods: Patients from the French GD Registry with information on the prese
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::66335a104c7bdecda5398e216cec9305
https://hal.archives-ouvertes.fr/hal-02304006
Zobrazit plný text záznamu
7
[Clostridium difficile infection in a Department of Internal Medicine. A consecutive series of 45 patients]
Autor: Dominique, Bligny, Bérengère, Cador, Anne, Jolivet-Gougeon, Anne, Le Strat, Claire, Cazalets, Elisabeth, Laurat, Patrick, Jego, Jacques, Bouget, Bernard, Grosbois
Publikováno v: Annales de medecine interne. 153(5)
A retrospective study of 45 patients with Clostridium difficile infection over a 4-year period in a department of Internal Medicine.Mean age was 79 years; sex-ratio (F/M)=1.5; 38% of the patients had neurological or severe psychiatric disorders; 20%
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e11b6a01a419e051bfdbc2b257da2c3f
https://pubmed.ncbi.nlm.nih.gov/12442074
Zobrazit plný text záznamu
8
[Intermittent fever of neoplastic origin]
Autor: Bérengère, Cador-Rousseau, Claire, Cazalets-Lacoste, Bernard, Grosbois
Publikováno v: La Revue du praticien. 52(2)
Cancer and hemopathy account from 4.5% to 14% of causes of intermittent fever (IF). The tumoral etiology is loss frequent in IF than continues fever. The man physiopathologic mechanism is represented by secretion of cytokines from tumour cells. IF ma
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::99a4f6857f8c257c34f261e1b9e1d960
https://pubmed.ncbi.nlm.nih.gov/11915557
Zobrazit plný text záznamu

Vyhledávací nástroje:

Upřesnit hledání

Omezení vyhledávání
Plný text Recenzováno Digitální knihovna AV ČR
Zdroje